A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515049



Internal ID22573008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102772804..102776603hg38UCSC Ensembl
chrX:102027732..102031531hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975563
Supporting Variants
Samples
Known GenesLINC00630
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515049
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer